Run ID: ERR4814700
Sample name:
Date: 01-04-2023 13:26:34
Number of reads: 446013
Percentage reads mapped: 58.88
Strain: lineage4.3.3
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.3 | Euro-American (LAM) | mainly-LAM | None | 0.99 |
lineage4.3.3 | Euro-American (LAM) | LAM;T | RD115 | 0.99 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rrs | 1472644 | n.799C>T | non_coding_transcript_exon_variant | 0.4 | streptomycin |
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.58 | streptomycin |
rrs | 1473247 | n.1402C>A | non_coding_transcript_exon_variant | 0.55 | kanamycin, capreomycin, aminoglycosides, amikacin |
rrs | 1473329 | n.1484G>T | non_coding_transcript_exon_variant | 0.5 | kanamycin, capreomycin, aminoglycosides, amikacin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 6994 | c.-308C>T | upstream_gene_variant | 0.4 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7850 | c.549C>G | synonymous_variant | 1.0 |
gyrA | 8040 | p.Gly247Ser | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 490928 | p.Gly49Val | missense_variant | 0.29 |
ccsA | 619734 | c.-157C>A | upstream_gene_variant | 1.0 |
rpoB | 762879 | p.Met1025Leu | missense_variant | 0.33 |
rpoC | 762902 | c.-468C>T | upstream_gene_variant | 0.5 |
rpoC | 762911 | c.-459C>T | upstream_gene_variant | 0.62 |
rpoC | 762917 | c.-453C>T | upstream_gene_variant | 0.62 |
rpoC | 762920 | c.-450C>T | upstream_gene_variant | 0.62 |
rpoC | 762929 | c.-441G>T | upstream_gene_variant | 0.62 |
rpoC | 762944 | c.-426C>T | upstream_gene_variant | 0.56 |
rpoC | 762956 | c.-414G>T | upstream_gene_variant | 0.5 |
rpoC | 762962 | c.-408C>T | upstream_gene_variant | 0.44 |
rpoC | 762983 | c.-387C>T | upstream_gene_variant | 0.3 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 779379 | c.-899C>G | upstream_gene_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781760 | c.201T>C | synonymous_variant | 0.17 |
rpsL | 781766 | c.207C>T | synonymous_variant | 0.15 |
rpsL | 781772 | c.213C>T | synonymous_variant | 0.17 |
rpsL | 781796 | p.Met79Ile | missense_variant | 0.14 |
rpsL | 781802 | c.243G>C | synonymous_variant | 0.14 |
rpsL | 781805 | c.246G>T | synonymous_variant | 0.14 |
rpsL | 781811 | c.252C>T | synonymous_variant | 0.14 |
rpsL | 781814 | c.255C>T | synonymous_variant | 0.14 |
rpsL | 781817 | c.258G>T | synonymous_variant | 0.14 |
rpsL | 781829 | c.270G>C | synonymous_variant | 0.15 |
rpsL | 781832 | c.273T>C | synonymous_variant | 0.15 |
rpsL | 781838 | c.279G>T | synonymous_variant | 0.17 |
rplC | 800908 | p.Asn34Asp | missense_variant | 0.22 |
Rv1258c | 1406943 | c.397_398insGC | frameshift_variant | 0.25 |
Rv1258c | 1406946 | p.Ala132Gly | missense_variant | 0.25 |
Rv1258c | 1406948 | c.391_392delGC | frameshift_variant | 0.25 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472102 | n.257G>A | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472112 | n.267C>T | non_coding_transcript_exon_variant | 0.53 |
rrs | 1472113 | n.268T>C | non_coding_transcript_exon_variant | 0.53 |
rrs | 1472122 | n.277G>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472123 | n.278A>T | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472124 | n.279C>T | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.94 |
rrs | 1472155 | n.310C>T | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472160 | n.315C>T | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.81 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472344 | n.499C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472379 | n.534T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472400 | n.555C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472416 | n.571C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472422 | n.577T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472507 | n.662C>G | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472517 | n.672T>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472518 | n.673G>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.59 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472544 | n.699C>A | non_coding_transcript_exon_variant | 0.63 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.63 |
rrs | 1472558 | n.713G>A | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472566 | n.721G>A | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472569 | n.724G>A | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472579 | n.734G>T | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.98 |
rrs | 1472597 | n.752G>A | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472607 | n.762G>A | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472647 | n.802C>T | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472655 | n.810G>T | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472660 | n.815T>C | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472670 | n.825G>T | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472673 | n.828T>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472675 | n.830T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472677 | n.832C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472681 | n.837_838delTT | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472687 | n.842_843insC | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472690 | n.845C>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.61 |
rrs | 1472714 | n.869A>G | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.59 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472755 | n.910G>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472790 | n.945T>C | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.49 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.48 |
rrs | 1472824 | n.979T>A | non_coding_transcript_exon_variant | 0.9 |
rrs | 1472825 | n.980G>A | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472827 | n.982G>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472828 | n.983T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472892 | n.1047T>C | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472895 | n.1050C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472951 | n.1106T>C | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472952 | n.1107T>C | non_coding_transcript_exon_variant | 0.7 |
rrs | 1472953 | n.1108G>A | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472954 | n.1109T>C | non_coding_transcript_exon_variant | 0.1 |
rrs | 1472955 | n.1110C>T | non_coding_transcript_exon_variant | 0.7 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472973 | n.1128A>T | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472987 | n.1142G>A | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472989 | n.1144G>A | non_coding_transcript_exon_variant | 0.76 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.91 |
rrs | 1472992 | n.1147A>G | non_coding_transcript_exon_variant | 0.1 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.97 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.97 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.97 |
rrs | 1473081 | n.1236C>T | non_coding_transcript_exon_variant | 0.12 |
rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 0.97 |
rrs | 1473093 | n.1248C>T | non_coding_transcript_exon_variant | 0.95 |
rrs | 1473100 | n.1255G>A | non_coding_transcript_exon_variant | 0.94 |
rrs | 1473102 | n.1257C>T | non_coding_transcript_exon_variant | 0.93 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.93 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.93 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.93 |
rrs | 1473115 | n.1270G>T | non_coding_transcript_exon_variant | 0.8 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.94 |
rrs | 1473123 | n.1278A>T | non_coding_transcript_exon_variant | 0.11 |
rrs | 1473130 | n.1285G>A | non_coding_transcript_exon_variant | 0.16 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.97 |
rrs | 1473163 | n.1318C>T | non_coding_transcript_exon_variant | 0.11 |
rrs | 1473164 | n.1319C>A | non_coding_transcript_exon_variant | 0.11 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.93 |
rrs | 1473177 | n.1332G>A | non_coding_transcript_exon_variant | 0.12 |
rrs | 1473192 | n.1347A>G | non_coding_transcript_exon_variant | 0.11 |
rrs | 1473199 | n.1356delA | non_coding_transcript_exon_variant | 0.11 |
rrs | 1473205 | n.1360T>C | non_coding_transcript_exon_variant | 0.11 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 0.73 |
rrs | 1473259 | n.1414C>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1473270 | n.1425G>A | non_coding_transcript_exon_variant | 0.46 |
rrs | 1473276 | n.1431A>G | non_coding_transcript_exon_variant | 0.7 |
rrs | 1473291 | n.1446G>A | non_coding_transcript_exon_variant | 0.22 |
rrs | 1473301 | n.1456T>C | non_coding_transcript_exon_variant | 0.8 |
rrs | 1473305 | n.1460G>T | non_coding_transcript_exon_variant | 0.55 |
rrs | 1473316 | n.1471C>T | non_coding_transcript_exon_variant | 0.86 |
rrl | 1474864 | n.1207C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474883 | n.1226T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476141 | n.2484A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476153 | n.2496T>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476165 | n.2508T>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476194 | n.2537A>G | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476200 | n.2543A>T | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476201 | n.2544C>T | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476214 | n.2557G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476215 | n.2558C>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476245 | n.2588C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476252 | n.2595T>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476253 | n.2596A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476256 | n.2599A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476337 | n.2680C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.92 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.95 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.96 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.94 |
rrl | 1476429 | n.2772A>T | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.9 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476585 | n.2928A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476596 | n.2939C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476600 | n.2943A>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476608 | n.2951C>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476614 | n.2957A>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476616 | n.2959A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476619 | n.2962C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476628 | n.2971T>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476629 | n.2972C>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476633 | n.2976A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476664 | n.3007T>A | non_coding_transcript_exon_variant | 0.67 |
rpsA | 1834195 | c.654G>C | synonymous_variant | 0.18 |
rpsA | 1834210 | c.669C>T | synonymous_variant | 0.14 |
rpsA | 1834213 | c.672G>A | synonymous_variant | 0.14 |
rpsA | 1834219 | c.678C>G | synonymous_variant | 0.14 |
rpsA | 1834222 | c.681T>C | synonymous_variant | 0.14 |
rpsA | 1834225 | c.684C>G | synonymous_variant | 0.15 |
rpsA | 1834228 | c.687C>T | synonymous_variant | 0.23 |
rpsA | 1834231 | c.690T>C | synonymous_variant | 0.15 |
rpsA | 1834246 | c.705G>T | synonymous_variant | 0.21 |
rpsA | 1834249 | c.708T>C | synonymous_variant | 0.21 |
rpsA | 1834252 | c.711C>T | synonymous_variant | 0.15 |
rpsA | 1834261 | c.720A>G | synonymous_variant | 0.3 |
rpsA | 1834264 | c.723G>C | synonymous_variant | 0.27 |
rpsA | 1834285 | c.744G>C | synonymous_variant | 0.2 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2103090 | c.-48G>T | upstream_gene_variant | 0.14 |
Rv1979c | 2222989 | p.Gly59Asp | missense_variant | 0.33 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518438 | c.325delG | frameshift_variant | 0.29 |
kasA | 2518919 | p.Gly269Ser | missense_variant | 1.0 |
pepQ | 2860240 | p.Tyr60Cys | missense_variant | 0.12 |
Rv2752c | 3065824 | p.Pro123Leu | missense_variant | 1.0 |
thyA | 3073868 | p.Thr202Ala | missense_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
Rv3083 | 3448854 | c.351C>A | synonymous_variant | 0.15 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
whiB7 | 3568773 | c.-94G>C | upstream_gene_variant | 0.33 |
alr | 3840265 | p.Ile386Val | missense_variant | 0.11 |
clpC1 | 4038287 | c.2418C>T | synonymous_variant | 1.0 |
clpC1 | 4040546 | c.159G>A | synonymous_variant | 0.18 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4249371 | p.Leu953Gln | missense_variant | 0.11 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407865 | c.337delG | frameshift_variant | 1.0 |
gid | 4408156 | p.Leu16Arg | missense_variant | 1.0 |